Canonical Allele Identifier: CA375415195
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133644228-A-C
MyVariant Identifiers: chr9:g.136509350A>C (hg19) chr9:g.133644228A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644228A>C , CM000671.2:g.133644228A>C GRCh38
NC_000009.11:g.136509350A>C , CM000671.1:g.136509350A>C GRCh37
NC_000009.10:g.135499171A>C NCBI36
NG_008645.1:g.12866A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.932A>C MANE Select ENSP00000376776.2:p.Tyr311Ser
ENST00000393056.6:c.932A>C ENSP00000376776.2:p.Tyr311Ser
NM_000787.3:c.932A>C NP_000778.3:p.Tyr311Ser
NM_000787.4:c.932A>C MANE Select NP_000778.3:p.Tyr311Ser
Search 100 bp 5'
Search 100 bp 3'